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My first post, so let me introduce myself, in case it helps someone who’s closer to the beginning of this difficult journey. I’ve had RRMS for over 20 years and been on DMTs for around 15. I’m still walking and working, but get tired easily, and I still drive, just with a blue badge in the car. So,...

I am now the happy owner of a BRIGHT SHINY left sided optic neuritis episode, confirmed by MRI. 💥🎉 Thankfully, I can now move up to more effective DMTs. I have the choice of Ocrevus(6 monthly infusions), Kesimpta(monthly injections at home) or Tysabri (monthly infusions). I'm looking for honest...

Can we link up? I want meet some London MSers..

Good evening Ladies, gentlemen & fellow hot MSers! I’ve discovered a chill tube! It’s under £10 online.. it’s like an ice pop type thing that is reusable.. freeze it and pop it round your neck! The coldness doesn’t last for too long, but certainly helps you to cool down! I’m over the moon with min...

Am I the one that reads this message on some forum posts? Well it has been fun contributing to the odd posts. Good luck to all you MSers out there. 🤝

Hello my dear MS fighter friends 🙂 Today I woke up with a strange thought. I'm jealous about health condition. Not thinking about "Why me? Why I have MS?" I'm jealous about those MSers who have RRMS. Because with my PPMS now is harder to fight than with my RRMS before. Strange thought I know, don...

Hello fellow MSers!! I am wondering if anyone on Kesimpta has noticed if their sensitivity to things like poison ivy/detergents/environmental allergens has gone haywire in the first few months of the drug? I have always had sensitive skin, yet no reaction to the ivys/oaks/sumacs. I'm wondering if t...

Hi all just asking if anyone, was moved from Tysabri to Tyruko? Last year October I had no choice but to change DMT, unfortunately for me I’ve had severe adverse affects, including one hospital admission considering I haven’t had an MS admissions in over 4 years, Luckily my hospital was able to c...